Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.739039
Title: A study of the role of splenic mesenchyme-to-epithelial transition in islet neogenesis
Author: Robertson, Stuart
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2010
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Abstract:
Type 1 Diabetes Mellitus (T1DM) affects millions of children worldwide and is increasing in prevalence. Exogenous insulin therapy is currently the mainstay of treatment but is unable to prevent the chronic complications of this disease. Islet transplantation is a successful, minimally-invasive, potentially curable alternative treatment, which has restored physiological euglycaemia in up to 85% of recipients in recent clinical trials. However, worldwide human donor islet shortages limit the wider application of this treatment. Pluripotent cells may provide alternative islet sources to overcome this shortage. The human spleen may be one such source and is an excellent candidate tissue for further investigation. The main aims of this thesis were to investigate whether the developing spleen could differentiate into insulin-producing cells and to investigate the molecular mechanisms behind this. Using an avian model of pancreatic development, I characterise normal avian foregut expression of the splenic mesenchymal transcription factor Tlx-1 between E4-E11 of development and report an optimised in situ hybridisation protocol for this. I use a chick-quail chimaera model of pancreatic organogenesis to show that the developing avian spleen is able to differentiate into insulin-producing cells in vitro through islet Mesenchyme-to-Epithelial Transition (iMET). 1 show evidence that, when recombined with differentiating pancreatic epithelium, splenic mesenchyme is reprogrammed to express the pancreatic islet genes Pdx-1 and Isl-1. Tlx-1 is dramatically down-regulated during this process, indicating that this tissue is reprogrammed from a splenic to pancreatic endocrine fate. Finally, an attempt to augment splenic iMET is made through the addition of a Wnt agonist. These findings, together with the recent discovery that the mature human spleen contains Tlx-1 positive cells, may be a useful target for future bench-to-bedside translation strategies for this work. Therefore, the spleen may be an ideal future tissue source for islet transplantation to treat patients with T1DM.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (M.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.739039  DOI: Not available
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